Tag | Content |
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EnhancerAtlas ID | HS118-01106 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr1:147279580-147281030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr1:147280054-147280065 | TTAATTAAAAT | - | 6.62 | Stat6 | MA0520.1 | chr1:147280420-147280435 | GATTTCCTGAGAATA | + | 6 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATAAGGGGG CTTCAAAAAC AAACTAGTCG TGTGGCCTGC CCCAGCATGT GGGCCTGACC 60 AAAACAATCC TATATATAGG CACTCTCTTA CCTTCCTTAG CATTGCAACC TATTGCGTTA 120 ATACCAGGCC CTCAGGCATC ACAGCGCCTC TGTCTCTCTA GACCATCTCC AGCCACTACC 180 TTCACCCGAC TTACAATTCA GCTAAACTCA ACTACTGTGT CTTTGCTTGT GCTGTTTCTT 240 TCCTGCCTCT TCCTCAAGTG GCTCCCACTT TGCATTCAAG ACTCAGCTCT TGTGTCTGGA 300 AACCTTTTAA ATCATTTCTC CCAAGCTGAG CATTGAGCCC TCCTCTGTGT GACTACAAGC 360 CTATACTTAC TTATTGTATA CAGCTTAGCA CTTTTAATAT TAGTTGGTAC AAAATTAATT 420 GTGGTTTTGG ACCGTGAATT TTAAACATTG TAACTAGGCT CAAACACTTC TTTATTAATT 480 AAAATAAGAA CCATTACAAT CAACATATTT TTGCCAATGA GAAGCAAATT TGTTTATTCC 540 TGTAGCATAA AAAATCTGTG CTTTGGGATT CAACAACTCT TGGAAAGTAC TTTCTGCATC 600 CTGCTGATTG TGGAAGCATT TCCCCTGCAA AAAGTTGTCA AAATGCTTGA AGAAGTGGTA 660 GTCAGTTGGC AAGAGGTCAG GTGAATATGG TGGATGAGGC AATACTTCAA AGCCCAATTC 720 GTTTATCTTT TGAAGCACTG GTTGTGCAAC CTGCAGTCGG GGGTTGTCAT GGAGAGGAAT 780 TTGGCCCTTT CTGTTAACTG ATGCCAGCTG CAGGCTTTGC AGTTTTCAGT GCATTTCATC 840 GATTTCCTGA GAATAGTTCT CAGATGTAAT GGTTTCTGGG ATTCAGAAAG CTGTAGTGGG 900 TCAGACTGGC AGACCACCAA ACAGTGACCA CGACTTTTTT TGGTGCAAGT TTGGCTTTGG 960 GAGGTGCTTT GGACCTTCTT CCCCATCCAA CCACTGAGTT GTCATCACCG ATTGTCATAT 1020 AAAATCCACT TTTCGAAGTA TGTCACAATC TGATCGAGAA ATGGTTCGTT GTTGTTGCAT 1080 AGAATAAAAT GATGGTTCAC AATGATGATT TTTAAAATTT TCACTGAACT CATGAGACAC 1140 CCACTTTTCC AGCTTTTTCA CCTTTCCAAT TTGCTTCAAA GGCTGAACGA CCATAGAATG 1200 GTCAACATGG AGTTCTTCAG CAACTTCTTG TGTAATTGTA AGAGGATCGG CTTTGACGAT 1260 TGCTCTCAAT TGGTCGTTGT CAACTTCCAA TGCCAAGACA CTATGCACCT CATCTTCAAG 1320 GCTCTCATCT CCTTTGCAAA ATTTCTTGAA CCAACACTGC ACTGCATGTT CATTAGCAGT 1380 TCCTAGCCAA ATGTGTTGTT GATGTTGTGA GTTGTCTGCA CTGCTTTACG ACCTATTTTG 1440 AACTCAAATA 1450
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